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Clinical Trials Advisor (CTA) is designed especially for the clinical trials professional charged with gathering submission-quality data while protecting the safety and welfare of study subjects.
With 12 issues a year, you can be confident that you'll stay abreast of the latest developments in global clinical trial trends, changes in trial endpoints and regulations that govern drug and medical device clinical trials.
Each issue of Clinical Trials Advisor provides:
Your subscription also includes access to The Clinical Trials Advisor Regulatory Resource Center — a one-stop location for all the guidance, regulation and laws you’ll need to comply with U.S and international clinical trial requirements. The resource center is updated continuously and available to you around the clock.
Monthly, 12 issues/year. Electronic delivery.
Renew Clinical Trials Advisor NOW and receive a FREE copy of our webinar, Reporting Failed Trial Data: New Rules for ClinicalTrials.gov — a $287 value. Also receive a FREE copy of our management report, Implementing e-Consent for Clinical Trials — a $397 value!
LINKS TO KEY DOCUMENTS — Need to read regulatory references, guidances, enforcement actions, and other documents? Simply click on the source documents in your electronic issue.
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